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Detecting genes associated with antimicrobial resistance and pathogen virulence in three New Zealand rivers

The emergence of clinically significant antimicrobial resistance (AMR) in bacteria is frequently attributed to the use of antimicrobials in humans and livestock and is often found concurrently with human and animal pathogens. However, the incidence and natural drivers of antimicrobial resistance and...

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Autores principales: Davis, Meredith, Midwinter, Anne C., Cosgrove, Richard, Death, Russell G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8647715/
https://www.ncbi.nlm.nih.gov/pubmed/34950535
http://dx.doi.org/10.7717/peerj.12440
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author Davis, Meredith
Midwinter, Anne C.
Cosgrove, Richard
Death, Russell G.
author_facet Davis, Meredith
Midwinter, Anne C.
Cosgrove, Richard
Death, Russell G.
author_sort Davis, Meredith
collection PubMed
description The emergence of clinically significant antimicrobial resistance (AMR) in bacteria is frequently attributed to the use of antimicrobials in humans and livestock and is often found concurrently with human and animal pathogens. However, the incidence and natural drivers of antimicrobial resistance and pathogenic virulence in the environment, including waterways and ground water, are poorly understood. Freshwater monitoring for microbial pollution relies on culturing bacterial species indicative of faecal pollution, but detection of genes linked to antimicrobial resistance and/or those linked to virulence is a potentially superior alternative. We collected water and sediment samples in the autumn and spring from three rivers in Canterbury, New Zealand; sites were above and below reaches draining intensive dairy farming. Samples were tested for loci associated with the AMR-related group 1 CTX-M enzyme production (bla(CTX-M)) and Shiga toxin producing Escherichia coli (STEC). The bla(CTX-M) locus was only detected during spring and was more prevalent downstream of intensive dairy farms. Loci associated with STEC were detected in both the autumn and spring, again predominantly downstream of intensive dairying. This cross-sectional study suggests that targeted testing of environmental DNA is a useful tool for monitoring waterways. Further studies are now needed to extend our observations across seasons and to examine the relationship between the presence of these genetic elements and the incidence of disease in humans.
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spelling pubmed-86477152021-12-22 Detecting genes associated with antimicrobial resistance and pathogen virulence in three New Zealand rivers Davis, Meredith Midwinter, Anne C. Cosgrove, Richard Death, Russell G. PeerJ Ecology The emergence of clinically significant antimicrobial resistance (AMR) in bacteria is frequently attributed to the use of antimicrobials in humans and livestock and is often found concurrently with human and animal pathogens. However, the incidence and natural drivers of antimicrobial resistance and pathogenic virulence in the environment, including waterways and ground water, are poorly understood. Freshwater monitoring for microbial pollution relies on culturing bacterial species indicative of faecal pollution, but detection of genes linked to antimicrobial resistance and/or those linked to virulence is a potentially superior alternative. We collected water and sediment samples in the autumn and spring from three rivers in Canterbury, New Zealand; sites were above and below reaches draining intensive dairy farming. Samples were tested for loci associated with the AMR-related group 1 CTX-M enzyme production (bla(CTX-M)) and Shiga toxin producing Escherichia coli (STEC). The bla(CTX-M) locus was only detected during spring and was more prevalent downstream of intensive dairy farms. Loci associated with STEC were detected in both the autumn and spring, again predominantly downstream of intensive dairying. This cross-sectional study suggests that targeted testing of environmental DNA is a useful tool for monitoring waterways. Further studies are now needed to extend our observations across seasons and to examine the relationship between the presence of these genetic elements and the incidence of disease in humans. PeerJ Inc. 2021-12-03 /pmc/articles/PMC8647715/ /pubmed/34950535 http://dx.doi.org/10.7717/peerj.12440 Text en © 2021 Davis et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.
spellingShingle Ecology
Davis, Meredith
Midwinter, Anne C.
Cosgrove, Richard
Death, Russell G.
Detecting genes associated with antimicrobial resistance and pathogen virulence in three New Zealand rivers
title Detecting genes associated with antimicrobial resistance and pathogen virulence in three New Zealand rivers
title_full Detecting genes associated with antimicrobial resistance and pathogen virulence in three New Zealand rivers
title_fullStr Detecting genes associated with antimicrobial resistance and pathogen virulence in three New Zealand rivers
title_full_unstemmed Detecting genes associated with antimicrobial resistance and pathogen virulence in three New Zealand rivers
title_short Detecting genes associated with antimicrobial resistance and pathogen virulence in three New Zealand rivers
title_sort detecting genes associated with antimicrobial resistance and pathogen virulence in three new zealand rivers
topic Ecology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8647715/
https://www.ncbi.nlm.nih.gov/pubmed/34950535
http://dx.doi.org/10.7717/peerj.12440
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